C. Bennett

发表

CCAAT/enhancer binding protein α, β and δ gene variants: associations with obesity related phenotypes in the Leeds Family Study

J. Barrett, A. Carter, L. Mccormack, 2010, Diabetes & vascular disease research.

Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause

M. Weedon, A. Swerdlow, M. Schoemaker, 2016, Human reproduction.

Genetic variation at the interleukin-1 locus is a determinant of changes in soluble endothelial factors in patients with acute coronary syndromes.

N. Camp, D. Crossman, S. Francis, 2002, Clinical science.

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency

A. Ashworth, N. Orr, A. Swerdlow, 2013, Genetics in Medicine.

Developing a tool to support diagnostic delivery of dementia

N. Moghaddam, Danielle De Boos, C. Bennett, 2019, Dementia.

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

A. Ashworth, J. Perry, M. Weedon, 2010, Human molecular genetics.

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure.

P. Jacobs, A. Murray, G. Conway, 2010, Human reproduction.

Reproductive genetics Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

P. Jacobs, A. Murray, G. Conway, 2010 .

FAMILIAL DEMENTIA IN RELATION TO THE 144 BP INSERT AND ITS IMPLICATIONS

Martin O. Leach, T. J. Crow, Mark Poulter, 1992 .